P. Jayamurugan, V. Ponnuswamy, S. Ashokan, R. Jayaprakash, N. Ashok, K. Guna and R. Mariappan
DBSA doped polypyrrole was prepared by In-situ chemical oxidative polymerization method. The reaction temperature was 0 to 20 °C. Different weight percentages of PSS (40 wt.%, 60 wt.% and 80 wt.%) were mechanically blended with a pestle in an agate mortar for 25 minutes by solid state mixing. The investigation of the blend focused on the optical, structural and morphological properties. SEM micrographs indicated that PSS was homogeneously distributed within DBSA doped PPy. FT-IR study confirmed the doped and blended dopants in the composite structure. UV-study revealed the π → π* transition in benzenoid rings of DBSA and presence of PSS. The semi-crystalline nature of the composites improved with increasing the weight percentage of PSS.
Ali A. Aljubouri, Abdulqader D. Faisal and Wafaa K. Khalef
Single phase, adherent films of copper oxide nanowires (CuO NWs) were successfully grown on a glass substrate. Titanium nanofilm was pre-coated on the glass substrate to assist the growth of a layer adherent to the substrate. The copper film of 1.5 μm thickness was deposited via physical vapor deposition technique followed by thermal oxidation in air at various temperatures for 4 h. The product was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), ultraviolet-visible (UV-Vis) and Fourier transformation infrared (FT-IR) spectroscopy to find the crystal structure, morphology, phases, and optical properties of the deposited films. The CuO NWs film with 60% transmittance at wavelengths greater than 800 nm was obtained. It can be used as an infrared thermal imaging filter and in optoelectronic devices. The fabricated temperature sensor exhibited high sensitivity in the temperature range of 20 °C to 180 °C.
R. Vasanthakumar, W. Nirmala, R. Santhakumari, R. Meenakshi and A. Sinthiya
4-aminopyridinium adipate monohydrate (4APA) was grown by slow evaporation solution growth technique. The functional groups in the grown crystal were identified from FT-IR spectral evaluation. The optical properties together with transmittance of the grown crystal were obtained from UV-Vis spectroscopic study. The mechanical and thermal properties of the grown crystal were studied using Vickers microhardness and TGA/DTA analyses, respectively. Microhardness test revealed that 4-aminopyridinium adipate monohydrate crystal is a soft category material. The density functional method (DFT) was performed using B3LYP with the 6-311G (d,p) basis set. The electronic charge distribution, reactivity of the molecules and the molecular electrostatic potential (MEP) of the grown crystal were analyzed using the B3LYP method. The intermolecular interactions that exist in the crystal structure of the 4APA have also been investigated by Hirshfeld surface analysis. The nonlinear optical properties of the 4APA crystal were confirmed by Kurtz-Perry technique.
Maria-Viorica Ciocilteu, Andreea Gabriela Mocanu, Adriana Mocanu, Catalin Ducu, Oana Elena Nicolaescu, Valentin Costel Manda, Adina Turcu-Stiolica, Claudiu Nicolicescu, Razvan Melinte, Maria Balasoiu, Octavian Croitoru and Johny Neamtu
The main objective of this study was to synthesize hydroxyapatite-ciprofloxacin composites using a chemical precipitation method and to evaluate the properties and in vitro release profile of the drug from the hydroxyapatite-ciprofloxacin composites. Composite characterization was achieved by FT-IR, XRD and DLS. Ciprofloxacin determination was accomplished by HPLC, resulting in good incorporation efficiency of the drug (18.13 %). The in vitro release study (Higuchi model C = K t1/2 and Ritger-Peppas model, C = K t0.6) showed a diffusion-controlled mechanism. The antibacterial activity showed that the bacterial growth inhibition zones were approximately equal for the synthesis composites and for the mechanical mixture on the Staphylococcus aureus germ.
The use of hydroxyapatite, which is a biocompatible, bioactive and osteoconductive material, with ciprofloxacin, which has good antibacterial activity in this composite, makes it suitable for the development of bone grafts. Furthermore, the synthesis process allows a slow local release of the drug.
Potassium iodide (KI) doped potassium hydrogen phthalate (KHP) single crystals were grown by slow evaporation technique using millipore water as a solvent. The grown single crystals were analyzed by powder X-ray diffraction and the analysis confirmed that KI-doped KHP crystallizes in orthorhombic system with space group Pca21. The functional groups were identified by FT-IR technique which showed slight shift in vibrational frequencies, indicating inclusion of dopant into the crystal lattice. The UV-Vis spectral studies revealed the optical transparency of the doped crystals in the entire visible region. The optical band gap values were estimated from Tauc plots. Kurtz-Perry powder test was employed for second harmonic generation efficiency studies of the grown crystals.
B. Punithaveni, K. Thilagavathy, N. Muthukumarasamy, D. Nithyaprakash and M. Saravanabhavan
New organic single crystals of 2-amino-6-methylpyridinium 2-hydroxybenzoate (2A6M2H) were grown by slow evaporation solution growth technique at room temperature. The grown crystal structure was studied using single crystal XRD. Crystalline nature and phases were confirmed by powder XRD analysis. FT-IR study was used to identify the functional groups present in the compound. UV-Vis study revealed that the lower cut off wavelength of the crystal is at 350 nm. The dielectric studies indicated the low value of dielectric loss at high frequency. Mechanical properties of the crystals were studied using Vickers microhardness test. The Z-Scan studies were conducted for the crystal using He–Ne laser.
Omer Kaygili, Niyazi Bulut, Tankut Ates, Ismail Ercan, Suleyman Koytepe, Turgay Seckin, Cengiz Tatar, Bayram Gunduz and Hanifi Kebiroglu
In the present study, the dopant effect of Zn on the crystal structure, thermal properties and morphology of magnesium aluminate (MgAl2O4) spinel (MAS) structure was investigated. A pure and two Zn-containing MASs (e.g. MgAl1.93Zn0.07O4 and MgAl1.86Zn0.14O4) were synthesized for this purpose via a wet chemical method, and the as-prepared samples were characterized by X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy, differential thermal analysis (DTA), thermogravimetric analysis (TGA), scanning electron microscopy (SEM) and energy dispersive X-ray (EDX) spectroscopy techniques. It was found that the crystal structure, thermal properties and morphology of the MAS system change with the increase in the amount of Zn. MgO phase formation was observed. The values of the lattice parameter, unit cell volume and crystallite size increased, and the crystallinity percentage decreased. The morphology was also affected by adding of Zn.
S. Reena Devi, S. Suresh, S. Kalaiyarasi, M. Nizammohideen and R. Mohan Kumar
A novel 4-methylpyridinium 3-nitrophthalate (4MP3NP) was synthesized and the crystals were grown by using slow evaporation method. The structural data of the grown crystal was collected by single crystal X-ray diffraction. It revealed that the 4MP3NP crystal belongs to triclinic crystal system with a space group P1. Structure of the synthesized compound was established using SHELXL 97 program package. The crystalline nature and composition of the grown crystal was established using high resolution X-ray diffraction and FT-IR analyses. UV-Vis transmittance and photoluminescence studies revealed the optical transmission window and electronic transition mechanism of ions, respectively. The laser damage threshold of the grown crystal was estimated by Nd:YAG laser and these results were mutually related to specific heat capacity of the grown crystal. The third-order nonlinear optical susceptibility of the grown crystal was studied by Z-scan technique.
An organic single crystal of 4-chloroanilinium hydrogen (2R,3R)-tartrate monohydrate (4CAHT) was grown by slow evaporation solution growth technique at room temperature. Single crystal XRD study confirmed that the crystal belongs to monoclinic system with the space group P21. Powder XRD analysis confirmed the crystalline nature of the compound. The presence of various functional groups in the compound was revealed by FT-IR analysis. UV studies showed the absence of absorption in the entire visible region. To determine the thermal stability of the grown crystals it was subjected to thermogravimetric and differential thermal analyses. Microhardness and etching studies were also carried out for the crystal. The powder second harmonic generation efficiency of 4CAHT was tested by Kurtz and Perry powder technique and the relative SHG efficiency of 4CAHT was found to be 1.44 times greater than that of standard KDP.
Nanosized NaA zeolite was successfully synthesized by hydrothermal method using tetraethyl orthosilicate (TEOS) and aluminum isopropoxide (AIP) as the main raw materials. The surface modification of NaA zeolite was carried out by silane coupling agent 3-aminopropyltriethoxysilane (KH-550). The effects of silane coupling agent dosage, reaction temperature, reaction time, hydrolysis time and pH value on grafting rate of NaA zeolite were investigated in detail. The zeolites were characterized by XRD, SEM-EDS, FT-IR and TG-DTA. The results showed that the surface of NaA zeolite was modified successfully by KH-550. The optimal modification conditions obtained were as follows: the dosage of coupling agent in 95 % ethanol – 1.6 %, reaction temperature − 70 °C, reaction time – 2 h, hydrolysis time – 20 min, and pH value – 3.5. Under these conditions, the grafting rate of modified NaA zeolite was 3.95 %.